Tris(3,5-dihydrocarbyl-4-hydroxy phenyl)phosphates

ABSTRACT

ORGANIC MATERIAL IS STABILIZED BY THE ADDITION OF ATRIS(3,5 - DIHYDROCARBYL-4-HYDROXYPHENYL)PHOSPHATE, EITHER ALONE OR IN COMBINATION WITH A DIALKYLTHIODIALKANOATE. THIS INVENTION RELATES TO NEW 3,5-DIHYDROCARBYL-4-HYDROXYPHENYL PHOSPHATES AND THEIR USE AS ANTIOXIDANTS. MOST ORGANIC MATERIALS UNDERGO DEGRADATION IN THE PRESENCE OF OXYGEN. THIS DEGRADATION IS ACCERLERATED AT INCREASE TEMPERATURES. FREQUENTLY, HIGH TEMPERATURES ARE ENCOUNTERED DURING THE PROCESS OF THESE MATERIALS IN MANUFACTURING OPERATIONS AND THUS SOME FORM OF STABILIZER IS REQUIRED FOR MANY MATERIALS, EVEN DURING THE MANUFACTURING STAGE. OTHER MATERIALS, ARE NOT SUBJECT TO EXTREMES IN TEMPERATURE DURING MANUFACTURE, BUT EVEN THESE UNDERGO DEGRADATION ON AGING.

United States Patent Oflice 3,716,603 Patented Feb. 13, 1973 3,716,603 TRIS(3,5-DIHYDROCARBYL-4-HYDROXY PHENYL)PHOSPHATES Bernard R. Meltsner, Royal Oak, Mich., assignor to Ethyl Corporation, New York, NY. No Drawing. Filed Nov. 1, 1965, Ser. No. 505,982 Int. Cl. C071? 9/12; C08k 1/60; C10l 1/26 US. Cl. 260-953 7 Claims ABSTRACT OF THE DISCLOSURE An object of this invention is to provide an additive capable of preventing degradation of organic materials due to oxygen. A further object of this invention is to provide organic materials that are stable against the effects of elevated temperatures during manufacture and also stable during long periods of aging under use conditions. A particular object is to provide a polyolefin (e.g., polypropylene) of exceptional high-temperature stability and capable of resisting degradation due to oxygen during long periods of use. Other objects will become apparent from the following description of the invention.

The above and other objects are accomplished by providing as a new composition of matter tris(3,5-dihydrocarbyl-4-hydroxyphenyl)phosphates. These new compounds have the formula:

wherein R is selected from the group consisting of alphabranched alkyl radicals containing from 3 to 18 carbon atoms, alpha-branched aralkyl radicals containing from 8 to 18 carbon atoms and cycloalkyl radicals containing from 6 to 18 carbon atoms; and R is selected from the group consisting of alkyl radicals containing from 1 to 18 carbon atoms, aralkyl radicals containing from 7 to 18 carbon atoms, aryl radicals containing from 6 to 18 carbon atoms and cycloalkyl radicals containing from 6 to 18 carbon atoms.

The following compounds serve to illustrate these new phosphates.

tris 3-methyl-S-tert-butyl-4-hydroxyphenyl)phosphate tris (3-e}thyl-5-isopropyl-4-hydroxyphenyl phosphate tris 3 -methyl--cyclohexyl-hydroxyphenyl phosphate tris 3-n-propyl-5- (a-methylbenzyl) -4-hydroxyphenyl) phosphate tris(3-methyl-5-(a-methylbenzyl)-4-hydroxyphenyl) phosphate tris 3-methyl-5- a,ot-dimethylbenzyl -4-hydroxyphenyl phosphate tris(3-phenyl-5-tert-butyl-4-hydroxyphenyl)phosphate In a preferred embodiment of this invention both R; and R are alpha-branched hydrocarbyl radicals. Some representative examples of these compounds are:

tris 3,5 -diisopropyl-4-hydroxyphenyl phosphate tris 3,5 -dicyclohexyl-4-hydroxyphenyl) phosphate tris 3,5 -di-sec-butyl-4-hydroxyphenyl) phosphate tris (3-isopropyl-5 -tert-butyl-4-hydroxyphenyl) phosphate tris (3-tert-butyl-5- (a-methylbenzyl) -4-hydroxyphenyl) phosphate tris( 3-tert-butyl-5-cyclohexyl-4-hydroxyphenyl) phosphate tris( 3-tert-dodecyl-5-sec-octadecyl-4-hydroxyphenyl) phosphate tris (3 -tert-nonyl-5-sec-octyl-4-hydroxyphenyl phosphate In a more preferred embodiment of this invention both R and R are tertiary alkyl radicals. These may be illustrated by the following compounds.

tris 3 5-di-tert-amyl-4-hydroxyphenyl phosphate tris 3 ,5-di-tert-octyl-4-hydroxyphenyl) phosphate tris 3,5 -di-tert-dodecyl-4-hydroxyphenyl phosphate tris 3 S-di-tert-o ctadecyl-4-hydroxyphenyl) phosphate tris 3,5-dia, x.-dimethylbenzyl) -4-hydroxyphenyl) phosphate tris (3 -tert-butyl-5 -tert-octyl-4-hydroxyphenyl) phosphate tris 3-tert-butyl-5- a,a-dimethylbenzyl) -4-hydroxyphenyl) phosphate tris(3-tert-amyl-5-tert-octadecyl-4-hydroxyphenyl phosphate In a most preferred embodiment of this invention the tris(3,5 dihydrocarbyl 4 hydroxyphenyl) phosphate is tris 3,5 -di-tert-butyl-4-hydroxyphenyl phosphate.

In the foregoing description many of the preferred R and R radicals are referred to as alpha-branched radicals." These are radicals wherein the carbon atom through which the radical bonds to the benzene ring is also bonded to at least two carbon atoms other than the carbon atom in the benzene ring. 'In other words, alpha-branched radicals are those commonly referred to as secondary or tertiary radicals such as the isopropyl and tert-butyl radicals.

The additive compounds of this invention are readily prepared by reacting a 2,6-dihydrocarbyl-p-hydroquinone with a phosphorus oxyhalide. Although any of the phosphorus oxyhalides may be employed, the preferred reactants are phosphorus oxybromide and phosphorus oxychloride and especially phosphorus oxychloride because of its low cost, availability and excellent results obtained with its use.

The 2,6-dihydrocarbyl-p-hydroquinones can be prepared by any of the methods available in the art such as the oxidation of the corresponding 2,6-dihydrocarbylp-aminophenol to the 2,G-di-hydrocarbyl-benzoquinone followed by reduction to the 2,6-dihydrocarbyl-p-hydroquinone. An especially useful method for preparing the preferred hydroquinones is through the air oxidation of the proper 2,6-di-tert-alkyl-4-tert-butylphenol. The air oxidation of such compounds leads to 2, 6-di-tert-alkyl p-benzoquinones which are readily converted to the corresponding hydroquinone by reduction. This method is described in detail in co-pending application Ser. No. 203,445, filed June 19, 1962 now US. Pat. No. 3,213,114.

The stoichiometry of the reaction requires three moles of the 2,6-dihydrocarbyl-p-hydroquinone per mole of phosphorus oxyhalide. Slightly more or slightly less of the hydroquinone can be employed. A preferred range is from about 2.8 to 3.1 moles per mole of phosphorus oxyhalide. A most preferred range is from about 2.9 to 3 moles of 2,6-dihydrocarbyl-p-hydroquinone per mole of phosphorus oxyhalide.

The reaction between the hydroquinone and the phosphorus oxychloride can be conducted by adding the phos phorus oxychloride to the hydroquinone or by adding the hydroquinone to the phosphorus oxychloride. The preferred method is to add the phosphorus oxychloride to the hydroquinone in a mole ratio of about one mole of phosphorus oxychloride to 3 moles of the hydroquinone, thus avoiding any excess of phosphorus oxychloride which might undergo undesirable side reactions with the tris- (3,5-dihydrocarbyl-4-hydroxyphenyl)-phosphate by way of chlorinating the phosphate or reacting with the hydroxyl substituent on the phosphate.

The reaction may be conducted in the presence or absence of a solvent. Usually it is preferred to employ a solvent because this makes it easier to moderate the reaction and also to purify the product. Preferred solvents are those in which the reactants are soluble and which are inert to the reactants or products under the reaction conditions. Some examples of these are ethers such as diethyl ether, ethyl butyl ether, di-n-propyl ether, ethylene glycol diethyl ether, diethyleneglycol dimethyl ether, and the like; esters such as ethyl acetate, amyl acetate, ethyl butyrate, and the like; and hydrocarbons such as hexane, heptane, isooctane, kerosene, petroleum ether (mixtures of low boiling hydrocarbons), mineral spirits, and the like. The more preferred solvents are hydrocarbons having a boiling point of from about 50 to about 200 C. Still more preferred hydrocarbon solvents are the aromatic hydrocarbons having a boiling point of from about 80 to about 200 C. Some examples of highly preferred solvents are toluene and xylene.

The reaction should be conducted at a temperature high enough so that the reaction proceeds at a reasonable rate, but not so high as to cause degradation of the product. A preferred temperature range is from about zero de grees up to about 200 C., and a most preferred temperature range is from about to C.

The reaction involves the evolution of a hydrogen halide, for example, HCl, and thus can be conducted in the presence of a hydrogen halide acceptor. Especially suitable hydrogen halide acceptors are the tertiary amines such as pyridine or triethylamine.

The reaction may be conducted in the presence of air, although it is usually preferred to carry the reaction out under a relatively inert atmosphere. An inert atmosphere removes the danger of explosions, minimizes the danger of solvent vapor explosions and lessens the likelihood of contaminating the product through oxidation. Although the process can be conducted at temperatures both below and above atmospheric pressure it is normallylconducted at atmospheric pressure.

The addition of the phosphorus oxyhalide to the 2,6- dihydrocarbyl-p-hydroquinone usually takes from about 15 minutes to several hours, depending upon the size of the reaction and the efficiency of heat removal. The addition time is not critical and can be carried out at as high a rate as permitted by the cooling means available; Under normal conditions the addition is readily com: pleted in from about 30 minutes to an hour- Preferably, the reaction is stirred at the reaction temperature for a short period following the completion of the additionof the reactants. Under most circumstances the reaction is complete in from about 0.5 to 8 hours following com pletion of addition. A preferred reaction time is from about one to 4 hours, and a most preferred reaction time is from about 2 to 3 hours.

The product may be recovered by any of the means known tothose skilled in the art. One useful method employed when a tertiary amine hydrogen halide acceptor is employed is to first filter off the tertiary amine hydrogen halide complex, following which all solvent is' distilled from the filtrate, leaving a semi liquid residue. This residue is then dissolved in a hot aliphatic hydrocarbon such as hexane and, upon cooling, the tris(3,5-dihydrocarbyl-4-hydroxyphenyl) phosphate will crystallize in high purity and good yield.

When the reaction is conducted without an amine hydrogen halide acceptor, the reaction mass can be merely washed with water at the end of the reaction period to remove any residual hydrogen halide. It is then preferably washed with a slightly basic solution (e.g., dilute Na CO solution) to neutralize any remaining acid.

When a high purity product is not required the product can be recovered by merely evaporating any solvent employed and using the residue as is. In still another embodiment the solution of the stabilizer may be used directly in blending with the organic materials requiring stabilization. Thus, when the reaction is conducted in a toluene solvent, the toluene solution of the stabilizer may be washed and neutralized to remove acidic material and then sprayed directly onto, for example, bulk polypropylene. The solvent is then evaporated off and the bulk polypropylene is ready for processing (e.g., molding, extrusion, and the like).

The following examples will serve to illustrate the preparation of the additive compounds of the present invention. All parts are parts by weight unless otherwise specified.

EXAMPLE 1 To a reaction vessel fitted with stirrer, thermometer, liquid addition means and cooling means was added 8.6 parts of 2,6-di-tert-butyl-p-hydro'quinone, 3.9 parts of triethylamine and 70 parts of diethyl ether. The vapor space above the liquid reactants was displaced with a nitrogen atmosphere which was maintained during the remainder of the reaction. A solution of 1.99 parts of phosphorus oxychloride in 18 parts of diethyl ether was added to the reaction vessel while stirring. The reaction temperature was maintained at about 30 C. during this addition. The

reaction was then stirred for about 12 hours, during which period a triethylamine hydrochloride precipitate formed. This precipitate was filtered off and the ether solvent was then removed from the filtrate by evaporation under vacuum (about 20 mm. Hg). The residue remaining was recrystallized from a methanol water mixture, giving White crystals having a melting point of 201-4 C. The infrared spectrum was consistent with that for tris(3,5-di-tert-butyl-4-hydroxyphenyl)phosphate. Analysis for carbon, hydrogen and phosphorus was carried out. The calculated analysis for tris(3,5-di-tert-butyl-4-hydroxyphenyl)phosphate is C, 70.96%; H, 8.93% and P, 4.36%. Found was C, 70.8%; H, 8.94% and P, 4.7%. Thus, the product was identified as tris(3,5-di-tert-butyl-4-hydroxypheuyl)phosphate.

EXAMPLE 2 To a reaction vessel equipped as in Example 1 is added 667 parts of 2,6-di-tert-butyl-p-hydroquinone and 1500 parts of toluene. Nitrogen is passed through the vessel until all air has been removed and a nitrogen atmosphere is maintained throughout the remainder of the reaction. While stirring, the vessel contents are heated to the reflux temperature of the solvent. While maintaining the reaction at reflux, 153.5 parts of phosphorus oxychloride are fed over a one hour period. Cooling is effected by reflux of the solvent. Following the phosphorus oxychloride addition, the reaction is refluxed for one additional hour. It is then allowed to cool and immediately upon dropping below C., 1000 parts of water are added to the reaction vessel and themixture stirred for 15 minutes. The water is drained off and the reactants are then washed with 1000 parts of a 5 percent sodium carbonatesolution. This solution is drained 01f and the toluene solvent is then removed by reducing the pressure in the reaction vessel to 50 mm. and slowly distilling out the toluene until the reaction vessel contents reach C. The remaining material is dissolved in a minimum amount of hot hexane and the hexane solution is then cooled to 0 C., causing the product to precipitate, forming a slurry.

The reaction mass is then filtered and the product, tris (3,5-di-tert-butyl 4 hydroxyphenyl)phosphate, is obtained.

EXAMPLE 3 To a reaction vessel equipped as in Example 1 is added 954 parts of 2,6-di(m-methyl-benzyl)-p-hydroquinone and 3000 parts of xylene. While stirring, 156 parts of phosphorus oxychloride are added over a period of 4 hours while maintaining the reaction temperature at 30 C. through external cooling. Following the phosphorus oxychloride addition, the reaction contents are stirred for 7 additional hours at 30 C. and then the temperature is slowly raised to 100 C. during an additional one hour period. The reaction mass is then cooled and washed twice with 1000 parts of water each. The reaction mass is then treated with 1000 parts of a percent sodium carbonate solution. Following this, the xylene solvent is removed by distilling out the solvent at 30 mm. of pressure until the reaction vessel attains a temperature of 150 C. The residue is recrystallized from a minimum quantity of petroleum ether (B.P. 6070 C.), yielding tris(3,5 di-(a-methylbenzyl)-4-hydroxyphenyl)-phosphate.

In the above example equal mole quantities of other 2,6-dihydrocarbyl-p-hydroquinones can be employed to give the corresponding tris(3,5-dihydrocarbyl-4-hydroxyphenyl)phosphate. For example, the use of 2,6-diisopropyl-p-hydroquinone yields tris(3,5-diisopropyl-4-hydroxyphenyl)phosphate. The use of 2,6-di-sec-butyl-p-hydroquinone yields tris(3,5-di-sec-butyl-4-hydroxyphenyl) phosphate. The use of 2,-di-tert-octyl-p-hydroquinone yields tris(3,5-di-tert-octyl-4 hydroxyphenyl)phosphate. The use of 2,6-dicyclohexyl-p-hydroquinone yields tris(3, 5-dicyclohexyl-4-hydroxyphenyl)phosphate. The use of 2, 6-di-tert-octadecyl-p-hydroquinone yields tris(3,5-di-tertoctadecyl-4-hydroxyphenyl)phosphate. The use of 2- methyl-6-(a,a-dimethylbenzyl)-p-hydroquinone yields tris [3-methyl-5-(a,a-dimethylbenzyl) 4 hydroxyphenyl] phosphate. The use of 2-(2,4-di-tert-butylphenyl)-6-tertdodecyl-p-hydroquinone yields tris[3-(2,4-di-tert butylphenyl -5-tert-dodecyl-4-hydroxypheny1] phosphate.

In like manner, equal mole quantities of other phosphorus oxyhalides can be used, such as phosphorus oxybromide, with good results.

The compounds of this invention are extremely useful as antioxidants in a wide variety of organic material normally susceptible to deterioration in the presence of oxy-- gen. Thus, liquid hydrocarbon fuels such as gasoline, kerosene and fuel oil are found to possess increased storage stability when blended with a stabilizing quantity of an additive of this invention. Likewise, hydrocarbon fuels contaning organometallic additives such as tetraethyllead, tetramethyllead, methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl nickel nitrosyl, ferrocene and iron carbonyl have appreciably increased stability when treated with the additives of this invention. Furthermore, lubricating oils and functional fluids, both those derived from naturally occurring hydrocarbons and those synthetically prepared, have greatly enhanced stability by the practice of this invention. The additives of this invention are extremely useful in stabilizing antiknock fluids against oxidative degradation. For example, the stabilizing additives of this invention find utility in stabilizing a tetraethyllead antiknock fluid which contains ethylenedichloride and ethylenedibromide.

The additives of this invention are effective in stabilizing rubber against degradation caused by oxygen or ozone. As used in the description and claims, the term rubber is employed in a generic sense to define a high molecular weight plastic material which possesses high extensibility under load coupled with the property of forcibly retracting to approximately its original size and shape after the load is removed. Some examples are acrylic rubber, butadiene-styrene rubber (SBR), chloroprene, chlorosulfonated polyethylene, fluorocarbon rubbers, isobutylene-isoprene (HR), isoprene, butadene, nitrile-butadiene rubber, polyisobutylene rubber, polysulfide rubbers, silicone rubbers, urethanes, India rubber, reclaimed rubber, balata rubber, gutta percha rubber, and the like. Both natural rubber and synthetic rubbers such as neoprene, SBR rubber, EPT rubber, GR-N rubber, chloroprene rubber, polyisoprene rubber, EPR rubber, and the like, are greatly stabilized through the practice of this invention.

The compounds of this invention are also useful in protecting pretroleum wax against degradation. The additives also find use in the stabilization of fats and oils of animal and vegetable origin which tend to become rancid during long periods of storage because of oxidative deterioration. Typical representatives of these edible fats and oils are linseed oil, cod liver oil, castor oil, soy bean oil, rapeseed oil, coconut oil, olive oil, palm oil, corn oil, sesame oil, peanut oil, babassu oil, butter, lard, beef tallow, and the like.

The compounds of this invention are superior antioxidants for high molecular weight polyolefins such as polyethylene (both high pressure and so-called Ziegler type polyethylene), polybutene, polybutadiene (both cis and trans), and the like.

One of the features of the present stabilizers is that they do not cause discoloration when used in transparent, white, or light-colored organic materials such as white rubber or plastics such as polyethylene, polypropylene, and the like.

The amount of stabilizer used in the organic composi tions of this invention is not critical, as long as a stabilizing quantity is present, and can vary from as little as 0.001 weight percent to about 5 weight percent. Generally, excellent results are obtained when from 0.1 to about 3 weight percent of the stabilizer is included in the organic compositions.

The following examples serve to illustrate the use of the stabilizers of the present invention in stabilizing some representative organic materials normally subject to deterioration in the presence of oxygen or ozone.

EXAMPLE 4 A rubber stock is prepared containing the following components:

Component: Parts Pale crepe rubber Zinc oxide filler 50 Titanium dioxide 25 Stearic acid 2 Ultramarine blue 0.12 Sulfur 3.00 Mercaptobenzothiazole 1.00

To the above base formula is added one part by weight of tris(3,S-di-tert-butyl-4-hydroxyphenyl)phosphate and, following this, individual samples are cured for 20, 30, 45 and 60 minutes, respectively, at 274 C. After cure, all of these samples remain white in color and possess excellent tensile strength. Furthermore, they are resistant to degradation caused by either oxygen or ozone on aging EXAMPLE 5 A synthetic rubber master batch comprising 100 parts of GR-S rubber having an average molecular weight of 60,000, 50 parts of mixed zinc propionate-stearate, 50 parts of carbon black, 5 parts of road tar, 2 parts of sulfur and 1.5 parts of mercaptobenzothiazole is prepared. To this is added 1.5 parts of tris-(3,5-(a-methylbenzyD-4- hydroxyphenyl) phosphate. This composition is then cured for 60 minutes employing 45 p.s.i.g. of steam pressure. The resulting synthetic rubber possesses resistance to oxygen and ozone induced degradation.

EXAMPLE 6 A butadiene acrylonitrile copolymer is prepared from 68 percent 1,3-butadiene and 32 percent acrylonitrile.

Two percent, based on the weight of the copolymer, of tris(3,S-diisopropyl-4-hydroxyphenyl)phosphate is added as an aqueous emulsion to the latex obtained from emul sion copolymerization of the rbutadiene and acrylonitrile monomers. The latex is coagulated with aluminum sulfate and the coagulum, after washing, is dried for 20 hours at 70 C. The synthetic copolyrner so obtained is resistant to oxidative degradation.

EXAMPLE 7 Three percent of tris(3,5-di-tert-octyl-4-hydroxyphenyl) phosphate as an emulsion in sodium oleate is added to a rubber-like copolymer of 1,3-butadiene and styrene containing 25 percent styrene. The resulting synthetic elastomer possesses enhanced stability.

EXAMPLE 8 To a master batch of GR-N synthetic rubber containing 100 parts of GR-N rubber, parts of zinc stearate, 50 parts of carbon black, 5 parts of road tar, 2 parts of sulfur and 2 parts of mercaptobenzothiazole is added 5 percent, based on weight, of tris(3,5-di-sec-butyl 4-hydroxyphenyDphosphate. After curing, a synthetic rubber is obtained of improved oxidative stability.

EXAMPLE 9 To a master batch of polyethylene having an average molecular weight of 1,000,000, a tensile strength of 6,700 p.s.i., a Shore D hardness of 74 and a softening temperature under low load of 150 C. is added 5 percent of tris(3,S-di-tert-butyl-4-hydroxyphenyl)phosphate. The resulting polyethylene possesses stability against oxidative degradation and shows no tendency to yellow after extensive aging.

EXAMPLE 10 A linear polyethylene having a high degree of crystallinity (93 percent), and less than one branched chain per 100 carbon atoms, a density of about 0.96 gram per ml. and which has about 1.5 double bonds per 100 carbon atoms, is mixed with 0.005 weight percent of tris(3,5-dicyclohexyl 4 hydroxyphenyl)phosphate. The resulting polyethylene is found to possess stability against oxidative degradation.

EXAMPLE 11 To 100 parts of an ethylenepropylene terpolymer is added 3 parts of tris(3-tert-amyl-5-tert-octyl-4-hydroxyphenyl)phosphate, resulting in an ethylenepropylene terpolymer of enhanced stability.

EXAMPLE 12 To 100 parts of an ethylenepropylene rubber is added 2 parts of tris(3-tert-nonyl-5-sec-octyl-4-hydroxyphenyl) phosphate, resulting in an EPR rubber stock of improved stability.

EXAMPLE 13 EXAMPLE 14 To 1,000 parts of a gasoline containing 26.6 percent aromatics, 20.8 percent olefins, 52.6 percent saturates and having an API gravity of 62.1 is added 10 parts of tris(3- tert butyl-5-cyclohexyl-4-hydroxyphenyl)phosphate. The resulting gasoline is stable.

EXAMPLE 15 To 10,000 parts of gasoline containing 8.6 percent aromatics, 7.9 percent olefins, 83.5 percent saturates and having an ARI gravity of 68.5 is added 200 parts of tris(3- methyl-5-cyclohexyl-4-hydroxyphenyl)phosphate. The resulting gasoline is stable against oxidative degradation.

EXAMPLE 16 To 10,000 parts of a gasoline containing 20.0 percent aromatics, 41.2 percent olefins, 38.8 percent saturates and containing additionally 1.5 grams of manganese per gallon as methyl cyclopentadientyl manganese tricarbonyl is added 300 parts of tris(3-phenyl-5-tert-butyl-4-hydroxyphenyl)phosphate. The resulting gasoline containing a manganese antiknock wasresistant to oxidative degradation.

EXAMPLE 17 To 10,000 parts of a gasoline containing 20.5 percent aromatics, 32.9 percent olefins and 46.6 percent saturates and containing 2.39 grams per gallon of tetraethyllead and one theory of chlorine as ethylenedichloride and 0.5 theory of bromine as ethylenedibromide is added 500 parts of tris(3,5-di-tert-butyl-4-hydroxyphenyl)phosphate. The resulting gasoline containing a lead antiknock and halogen scavenger is resistant to oxidative degradation. Not only this, but it is also found when used to give prolong spark plug life due to the presence of the phosphorus containing antioxidant.

EXAMPLE 18 To 10,000 parts of gasoline containing 38.1 percent aromatics, 7.3 percent olefins and 54.6 percent saturates and which contains 3.17 grams per gallon of lead as tetramethyllead, one theory of chlorine as ethylenedichloride, 0.5 theory of bromine as ethylenedibromide and 0.2 theory of phosphorus as tris(fl-chloroisopropyl)thionophosphate is added 50 parts of tris[3-tert-butyl-5-(a,adimethylbenzyl)-4-hydroxyphenyl]phosphate. The resulting gasoline is resistance to degradation and gives prolonged spark plug life on use.

EXAMPLE 19 An antiknock fluid composition is prepared by mixing together 61.5 parts of tetraethyllead, 17.9 parts of ethylenedibromide, 18.8 parts of ethylenedichloride and 1.3 parts of tris(3,5-di-tert-butyl-4-hydroxyphenyl)phosphate, resulting in a stable antiknock fluid composition.

EXAMPLE 20 To 1,000 parts of a commercial diesel fuel having a cetane number of 42, is added 5 parts of amyl nitrate and 4 parts of tris[3-n-propyl-5-(a-methylbenzyl)-4-hydroxyphenyl]phosphate, resulting in a diesel fuel of high resistance to oxidative deterioration which does not form gum or sludge on storage.

EXAMPLE 21 To 1,000 parts of a solvent refined neutral oil viscosityjndex and 200 SUS at F.) containing 6 percent of a commercial methacrylate type B-l improver is added 5 percent of tris[3,5-di-(a-methylbenzyl)-4-lrydroxyphenylJphosphate, resulting in a stable lubricating oil.

EXAMPLE 22 To a solvent refined crankcase lubricating oil having a viscosity index of 95 and a SAE viscosity of 10 is added 0.1 percent of tris (3,5-di-tert-dodecyl-4-hydroxyphenyl) phosphate. The resulting oil was stable against oxidative degradation.

9 EXAMPLE 23 To 100,000 parts of a commercially available pentaerythritol ester having a viscosity at 100 F. of 22.4

centistokes and known under the tradename of Hercofiex 600 is added 400 parts of tris(3,5-di-cyclohexyl-4- hydroxyphenyl)phosphate. The resulting synthetic lubricating oil possesses improved resistance against oxidative deterioration.

EXAMPLE 25 To 100,000 parts of dioctyl sebacate having a viscosity at 210 F. of 36.7 SUS, a viscosity index of 159, and a molecular weight of 427, is added 250 parts of tris- (3-phenyl-5-tert-butyl 4 hydroxyphenyl) phosphate, resulting in a synthetic diester lubricating oil having improved resistance to oxidative degradation.

EXAMPLE 26 To 1,000 parts of a commercial coconut oil is added 5 parts of tris[3-tert-butyl-5-(a-methylbenzyl)-4-hydroxyphenyl]phosphate, resulting in a vegetable oil with good aging characteristics.

EXAMPLE 27 To 100,000 parts of lard is added 100 parts of tris- (3-tert-butyl-5-cyclohexyl 4 hydroxyphenyl) phosphate, resulting in a lard having resistance to rancidity.

The stabilizing additives of this invention are eminently useful as stabilizers in polyolefins such as polyethylene, polypropylene, and the like. In this use they function as antioxidants, antiozonants and also as thermal stabilizers. They are extremely long lasting and highly resistant to the formation of color.

In order to demonstrate their vastly superior stabilization effect tests were conducted using a commercial polypropylene. These tests are known as Oven Aging Tests and are recognized in the plastic industry as an accurate guide to oxidative stability. In these tests small specimens of polypropylene are prepared containing the test stabilizer. These test specimens are placed in an air circulating oven maintained at 150 C. Five replicates are made of each polypropylene-stabilizer composition and the test criteria is the time and hours until three of the five replicates show signs of deterioration. Deterioration is evidenced by cracking, discoloration or any visual appearance of change in the specimen.

Test specimens are prepared by mixing the test stabilizers with polypropylene powder for 3 minutes in a Waring Blendor. The mixture is then molded into a 6" x 6" sheet with a thickness of either 0.025" or 0.0625". This is accomplished in a molding press at 400 F. under 5,000 p.s.i. pressure. Each sheet is then cut into /z" x 1" test specimens in order to obtain the five replicate samples. These samples are then subjected to the Oven Aging Tests.

In order to compare the stabilizing additives of this invention tests were carried out employing several commercially accepted stabilizers along with the preferred stabilizer of the present invention. The results obtained are shown in the following table.

Concen- Sample Hours tretion thickto (weight ness, tail- Additive percent) mils ure None 25 2. 5 2,6-dl-ter t-butyl-4-methylphenol 0. 3 25 16 2,2-methylenebis-(4-methyl-fi-tertbutylphenol) 0. 3 25 112 4,4'-thiobis(Z-tert-butyl-5-rnethylphenol) 0 3 25 96 'Iris(3,5-di-tert-butyl-t-hydroxyphenyl)- phosphate 0. 3 25 1, 648 Tris(3,fi-di-tert-butylt hydroxyphenyl)- phosphate 62 1, 76

As the above table shows, the additive of the present invention increased the oven life of the polypropylene almost 700 times that obtained without any additive, and about 17 times as much as the life obtained with two commercially accepted antioxidants. Thus, it can be seen that the additives of the present invention are vastly superior to stabilizers available in the prior art.

The etfectiveness of the present stabilizers can be enhanced still further by employing synergistic mixtures of the stabilizers of this invention. The preferred synergists are those having the formula:

wherein n is an integer from 1 to 5, and R is selected from the group consisting of alkyl radicals containing from 1 to 20 carbon atoms, aryl radicals containing from 6 to 20 carbon atoms, aralkyl radicals containing from 7 to 20 carbon atoms and cycloalkyl radicals containing from 6 to 20 carbon atoms. In the preferred synergist n is an integer from 1 to 3 and R is selected from the group consisting of alkyl radicals containing from 10 to 18 carbon atoms. The most preferred synergists are dilaurylthiodipropionate and distearylthiodipropionate.

The ratio of synergist to stabilizing compound should be adjusted to give the desired protection at the least cost. Mixtures containing from 1 percent synergist and 99 percent stabilizer to those containing 99 percent synergist and 1 percent stabilizer can be employed. Best results are usually obtained with stabilizing mixtures containing from 50 to 66 percent synergist and from 34 to 50 percent stabilizing compound.

The synergists can be employed to obtain increased stability using the same concentration of stabilizer or they can be employed to obtain the same stability with less of the stabilizer. Synergists are especially useful in this latter application. Thus, although dilaurylthiodipropionate (DLTDP) is only moderately effected by itself in stabilizing polypropylene, when used with a compound of the present invention a synergist interaction occurs, resulting in a degree of stability totally unexpected from the amount of stabilizers employed. This effect is shown in the following data obtained using the previously described Oven Aging Test.

Concen- Sample Hours tration thickto (weight ness, fail- Sarnple number percent) mils ure 1. None 62 2. 5 2. DLTDP 0.3 62 288 3. tris(3,5-ditert-butylA-hydroxyphenyl)- phosphate 0. 3 62 1, 768 4. tris(3,5-di-tert-butyl-4-hydroxyphenyl)- phosphate plus DLTDP 0. 1-0. 2 62 1,600

11 r r r Following are some examples of the synergistic stabilizing compositions of the present invention.

Tris(3 methyl 5 cyclohexyl 4 hydroxyphenyl) phosphate 99 Di n octyl thiodipropionate 1 Tris(3 methyl 5 (a methylbenzyl)-4-hydroxy phenyl)phosphate Didecylthiodiacetate 25 Tris(3 methyl 5 (:,0: dimethylbenzyl)-4-hy-' droxyphenyl)phosphate 25 Diundecylthiodibutyrate 75 Tris(3,5 dicyclohexyl 4 hydroxyphenyDphosphate 25 Dioctadecylthiodipropionate 75 Tris( 3 tert butyl (ot-methylbenzyl)-4-hydroxyphenyl)phosphate 80 Dinonadecythiodibutyrate 20 Tris( 3 tert dodecyl 5 sec octadecyl-4-hydroxyphenyl)phosphate 60 Dieicosylthiodipropionate 40 Tris (3,5 di tert butyl-4-hydroxyphenyl)phosphate Dilaurylthiodipropionate 90 Tris(3,5 di tert butyl 4 hydroxyphenyl) phosphate 90 Dilaurylthiodipropionate 10 Tris(3,5 di tert butyl 4 hydroxyphenyl) phosphate 30 Distearylthiodipropionate 70 The above synergistic stabilizer compositions are beneficially employed in any of the previously described organic materials normally susceptible to deterioration due to the effect of oxygen or ozone. In Examples 4 through 27, each of the above synergistic compositions can be substituted for the stabilizing compound of the present invention now shown, resulting in an organic composition of increased resistance to degradation from the efiects of oxygen or ozone.

; 12 What is claimed is:' 1. An antioxidant compound, said compound having the formula:

1 HO- 0 i 1 13 wherein R is selected from the group consisting of alphabranched alkyl radicals containing from 3 to 18 carbon atoms, alpha-branched aralkyl radicals containing from 8 to 18 carbon atoms and cyclohexyl radicals; and R is selected from the group consisting of alkyl radicals containing from 1 to 18 carbon atoms, aralkyl radicals containing from 7 to 18 carbon atoms, aryl radicals con -v taining from 6 to 18 carbon atoms and cyclohexyl radwherein R is alpha-branched alkyl containing 3 to 8 carcarbon atoms, alpha-branch aralkyl containing 8 to 9 carbon atoms and cyclohexyl; R is the same as R or alkyl of 1 to 18 carbon atoms.

References Cited UNITED STATES PATENTS 3,361,846 1/1968 Gleim et al 260953 U R LEWIS GOTTS, Primary Examiner A. H. SUTTO, Assistant Examiner U.S. Cl. X.R.

4476. BIG. 4; 252-49.8, 400; 260398.5, 481 R, 9 74 

